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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 903306생성일: 2026년 10월 26일

Acetic Acid → 2-(Trichloromethyl)oxazolidine

https://huagongshe.com/reaction/903306

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물EthanolamineHCID 700—
반응물ChloralHCID 6407—
반응물Sodium HydroxideHCID 14798—
용매TolueneHCID 1140—
생성물2-(Trichloromethyl)oxazolidineHCID 99029—

반응 단계

To a 2 liter 3-necked flask equipped with a stirrer, Dean-Stark trap, a condenser and dropping funnel were added 214 g (3.51 moles) ethanolamine and 450 g. toluene. Then 273 g (4.55 moles) of glacial acetic acid were added slowly to keep the temperature (cooling if necessary) at 30°-45° C. Then 568 g (3.85 moles) of chloral were added at 40°-50° C. The reaction mixture was refluxed to remove water and, when complete, the temperature increased to 115°-120° C. The reaction mixture was cooled in an ice bath and the product precipitated after standing for several hours to give 189.5 g (28.5%) m.p. 72°-74° C. The filtrate was washed with 5.0 moles of 20% sodium hydroxide and more product precipitated. Filtration and drying yielded 228.5 g (34.3%), m.p. 73°-75° C. The toluene layer was washed with water and evaporated to give a solid. Washing with water and filtration yielded upon drying 328 g. (49.2%), m.p. 62°-72° C. for a total yield of 556.0 g (83.5%). The analysis was consistent with the assigned structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04226948
출처 데이터셋uspto-grants-1980_10
ORD IDord-dc2019b6a5c54e4db5f086b11d45ad18
출처 메모uspto-grants-1980_10